(Q24682055)

English

The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption

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scholarly article

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The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption (English)

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1 reference

based on heuristic

inferred from title

hereditary folate malabsorption

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author name string

Rongbao Zhao

1

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Sang Hee Min

2

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Andong Qiu

3

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Antoinette Sakaris

4

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Gary L Goldberg

5

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Claudio Sandoval

6

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J Jeffrey Malatack

7

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David S Rosenblatt

8

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I David Goldman

9

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language of work or name

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publication date

15 August 2007

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110

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4

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1147-52

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Identification of an intestinal folate transporter and the molecular basis for hereditary folate malabsorption

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

7 April 2017

Identification and characterization of a lysosomal transporter for small neutral amino acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

7 April 2017

Identification of an intestinal heme transporter

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

7 April 2017

The SLC36 family: proton-coupled transporters for the absorption of selected amino acids from extracellular and intracellular proteolysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

7 April 2017

Balancing acts: molecular control of mammalian iron metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

7 April 2017

Micronutrient and urate transport in choroid plexus and kidney: implications for drug therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 September 2017

Autoantibodies to folate receptors in the cerebral folate deficiency syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 September 2017

Membrane transport of folates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 September 2017

Hereditary folate malabsorption: family report and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 September 2017

Congenital folate malabsorption

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 September 2017

The folate receptor works in tandem with a probenecid-sensitive carrier in MA104 cells in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 September 2017

Functional coupling between a bafilomycin A1-sensitive proton pump and a probenecid-sensitive folate transporter in human placental choriocarcinoma cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

30 May 2018

Structure and regulation of the murine reduced folate carrier gene: identification of four noncoding exons and promoters and regulation by dietary folates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 November 2018

A family study of congenital malabsorption of folate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 November 2018

Adaptive regulation of intestinal folate uptake: effect of dietary folate deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1939898

28 November 2018

Isolated congenital malabsorption of folic acid in a male infant: insights into treatment and mechanism of defect

1 reference

https://pubmed.ncbi.nlm.nih.gov/17446347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A combined TDDA-PVC pH and reference electrode for use in the upper small intestine

1 reference

https://pubmed.ncbi.nlm.nih.gov/17446347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-term treatment of congenital folate malabsorption

1 reference

https://pubmed.ncbi.nlm.nih.gov/17446347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of the amino acid 45 residue in reduced folate carrier function and ion-dependent transport as characterized by site-directed mutagenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17446347

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1182/BLOOD-2007-02-077099

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